Influenza-induced inflammation drives pneumococcal otitis media

Kirsty R Short, Patrick C Reading, Lorena E Brown, John Pedersen, Brad Gilbertson, Emma R Job, Kathryn M Edenborough, Marrit N Habets, Aldert Zomer, Peter W M Hermans, Dimitri A Diavatopoulos, Odilia L Wijburg

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    Influenza A virus (IAV) predisposes individuals to secondary infections with the bacterium Streptococcus pneumoniae (the pneumococcus). Infections may manifest as pneumonia, sepsis, meningitis, or otitis media (OM). It remains controversial as to whether secondary pneumococcal disease is due to the induction of an aberrant immune response or IAV-induced immunosuppression. Moreover, as the majority of studies have been performed in the context of pneumococcal pneumonia, it remains unclear how far these findings can be extrapolated to other pneumococcal disease phenotypes such as OM. Here, we used an infant mouse model, human middle ear epithelial cells, and a series of reverse-engineered influenza viruses to investigate how IAV promotes bacterial OM. Our data suggest that the influenza virus HA facilitates disease by inducing a proinflammatory response in the middle ear cavity in a replication-dependent manner. Importantly, our findings suggest that it is the inflammatory response to IAV infection that mediates pneumococcal replication. This study thus provides the first evidence that inflammation drives pneumococcal replication in the middle ear cavity, which may have important implications for the treatment of pneumococcal OM.

    Original languageEnglish
    Pages (from-to)645-52
    Number of pages8
    JournalInfection and Immunity
    Volume81
    Issue number3
    DOIs
    Publication statusPublished - 2013

    Keywords

    • Animals
    • Inflammation
    • Influenza A virus
    • Interleukin-6
    • Interleukin-8
    • Mice
    • Mice, Inbred C57BL
    • Orthomyxoviridae Infections
    • Otitis Media
    • Pneumococcal Infections
    • Viral Load

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